PT3555105T - Compostos de 7-feniletilamino-4h-pirimido[4,5-d][1,3]oxazin-2-ona como inibidores de idh1 e idh2 mutantes - Google Patents

Compostos de 7-feniletilamino-4h-pirimido[4,5-d][1,3]oxazin-2-ona como inibidores de idh1 e idh2 mutantes

Info

Publication number
PT3555105T
PT3555105T PT178228821T PT17822882T PT3555105T PT 3555105 T PT3555105 T PT 3555105T PT 178228821 T PT178228821 T PT 178228821T PT 17822882 T PT17822882 T PT 17822882T PT 3555105 T PT3555105 T PT 3555105T
Authority
PT
Portugal
Prior art keywords
phenylethylamino
pyrimido
oxazin
compounds
mutant idh1
Prior art date
Application number
PT178228821T
Other languages
English (en)
Portuguese (pt)
Original Assignee
Lilly Co Eli
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of PT3555105T publication Critical patent/PT3555105T/pt

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5365Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
PT178228821T 2016-12-16 2017-12-08 Compostos de 7-feniletilamino-4h-pirimido[4,5-d][1,3]oxazin-2-ona como inibidores de idh1 e idh2 mutantes PT3555105T (pt)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201662435283P 2016-12-16 2016-12-16

Publications (1)

Publication Number Publication Date
PT3555105T true PT3555105T (pt) 2020-12-21

Family

ID=60888651

Family Applications (1)

Application Number Title Priority Date Filing Date
PT178228821T PT3555105T (pt) 2016-12-16 2017-12-08 Compostos de 7-feniletilamino-4h-pirimido[4,5-d][1,3]oxazin-2-ona como inibidores de idh1 e idh2 mutantes

Country Status (37)

Country Link
US (3) US11001596B2 (ru)
EP (2) EP3763717B1 (ru)
JP (1) JP6793836B2 (ru)
KR (1) KR102276022B1 (ru)
CN (2) CN115109075B (ru)
AU (2) AU2017378060B2 (ru)
CA (1) CA3045303C (ru)
CL (1) CL2019001551A1 (ru)
CO (1) CO2019005287A2 (ru)
CR (1) CR20190252A (ru)
CY (1) CY1123577T1 (ru)
DK (1) DK3555105T3 (ru)
DO (1) DOP2019000163A (ru)
EA (1) EA036112B1 (ru)
EC (1) ECSP19042682A (ru)
ES (2) ES2941631T3 (ru)
HR (1) HRP20201882T1 (ru)
HU (1) HUE052067T2 (ru)
IL (1) IL267236B (ru)
JO (1) JOP20190142B1 (ru)
LT (1) LT3555105T (ru)
MA (2) MA53881A (ru)
MD (1) MD3555105T2 (ru)
MX (1) MX2019006830A (ru)
MY (1) MY197313A (ru)
NZ (1) NZ754115A (ru)
PE (1) PE20190977A1 (ru)
PH (1) PH12019501328A1 (ru)
PL (1) PL3555105T3 (ru)
PT (1) PT3555105T (ru)
RS (1) RS61108B1 (ru)
SA (1) SA519401897B1 (ru)
SI (1) SI3555105T1 (ru)
TN (1) TN2019000158A1 (ru)
UA (1) UA123640C2 (ru)
WO (1) WO2018111707A1 (ru)
ZA (1) ZA201903125B (ru)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9771349B2 (en) 2014-09-19 2017-09-26 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
ES2768694T3 (es) 2014-09-19 2020-06-23 Forma Therapeutics Inc Composiciones de quinolinona pirimidinas como inhibidores de isocitrato dehidrogenasa mutante
MY197533A (en) 2014-09-19 2023-06-21 Forma Therapeutics Inc Pyridin-2(1h)-one quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
AU2015317322B2 (en) 2014-09-19 2020-09-17 Forma Therapeutics, Inc. Phenyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US9624175B2 (en) 2015-04-21 2017-04-18 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10407419B2 (en) 2015-04-21 2019-09-10 Forma Therapeutics, Inc. Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors
US10131663B2 (en) 2016-10-24 2018-11-20 Astrazeneca Ab Chemical compounds
JOP20190144A1 (ar) 2016-12-16 2019-06-16 Janssen Pharmaceutica Nv إيميدازو بيرولو بيريدين كمثبطات لعائلة jak الخاصة بإنزيمات الكيناز
EP3763717B1 (en) * 2016-12-16 2023-03-08 Eli Lilly And Co. Pyrido[4,3-d][1,3]oxazin-2-one compounds as mutant idh1 and idh2 inhibitors
CA3046965A1 (en) 2016-12-16 2018-06-21 Janssen Pharmaceutica Nv Small molecule inhibitors of the jak family of kinases
DK3494116T3 (da) 2017-01-30 2020-01-27 Astrazeneca Østrogenreceptormodulatorer
US20210196701A1 (en) 2018-05-16 2021-07-01 Forma Therapeutics, Inc. Inhibiting mutant idh-1
US10532047B2 (en) 2018-05-16 2020-01-14 Forma Therapeutics, Inc. Solid forms of ((S)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile
US11311527B2 (en) 2018-05-16 2022-04-26 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
US11013734B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
US11013733B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1)
TW202016110A (zh) 2018-06-15 2020-05-01 比利時商健生藥品公司 Jak激酶家族之小分子抑制劑
EP4055015A1 (en) * 2019-11-08 2022-09-14 Nerviano Medical Sciences S.r.l. Gem-disubstituted heterocyclic compounds and their use as idh inhibitors
KR20220155378A (ko) 2020-03-23 2022-11-22 일라이 릴리 앤드 캄파니 돌연변이체 idh 억제제를 사용한 조합 요법
CA3172679A1 (en) 2020-03-23 2021-09-30 Nathan Arthur BROOKS Use of 7-phenylethylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one compounds for treating idh1 inhibitor-resistant subjects
KR20220156593A (ko) 2020-03-23 2022-11-25 일라이 릴리 앤드 캄파니 돌연변이체 idh 억제제 및 bcl-2 억제제를 사용한 조합 요법
WO2022001916A1 (zh) * 2020-06-28 2022-01-06 微境生物医药科技(上海)有限公司 Idh突变体抑制剂及其用途
EP4181927A1 (en) 2020-07-20 2023-05-24 Eli Lilly and Company Combination therapy with a mutant idh1 inhibitor, a deoxyadenosine analog, and a platinum agent
CN113588768B (zh) * 2021-05-18 2022-07-05 国家卫生健康委科学技术研究所 一种以分子图像方式定量组织内内源性代谢物的质谱方法
US20240261294A1 (en) 2021-06-09 2024-08-08 Eli Lilly And Company Method for treating idh inhibitor-resistant subjects
BR112023024454A2 (pt) * 2021-06-15 2024-02-06 Wigen Biomedicine Tech Shanghai Co Ltd Composto de fórmula geral (1) ou um isômero, uma forma cristalina, um sal farmaceuticamente aceitável, um hidrato ou um solvato do mesmo; e; uso do composto ou do isômero
CA3224704A1 (en) 2021-08-13 2023-02-16 David Andrew Coates Solid forms of 7-[[(1s)-1-[4-[(1s)-2-cyclopropyl-1-(4-prop-2-enoylpiper azin-1-yl)ethyl]phenyl]ethyl]amino]-1-ethyl-4h- pyrimido[4,5-d] [1,3]oxazin-2-one
WO2023141087A1 (en) 2022-01-19 2023-07-27 Eli Lilly And Company Combination therapy with a mutant idh inhibitor

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CU24269B1 (es) * 2011-09-27 2017-08-08 Novartis Ag 3- pirimidin- 4-il- oxazolidin- 2- onas inhibidores de la idh mutante
WO2014141153A1 (en) * 2013-03-14 2014-09-18 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
WO2014147586A1 (en) * 2013-03-22 2014-09-25 Novartis Ag 1-(2-(ethylamino)pyrimidin-4-yl)pyrrolidin-2-ones as inhibitors of mutant idh
US9624175B2 (en) * 2015-04-21 2017-04-18 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2016171715A1 (en) * 2015-04-24 2016-10-27 Halliburton Energy Services, Inc. Methods of fabricating ceramic or intermetallic parts
JP6473270B2 (ja) * 2015-07-27 2019-02-20 イーライ リリー アンド カンパニー 7−フェニルエチルアミノ−4h−ピリミド[4,5−d][1,3]オキサジン−2−オン化合物及び変異体idh1阻害剤としてのそれらの使用
JP6682043B2 (ja) * 2016-06-06 2020-04-15 イーライ リリー アンド カンパニー 変異体idh1阻害剤
EP3763717B1 (en) * 2016-12-16 2023-03-08 Eli Lilly And Co. Pyrido[4,3-d][1,3]oxazin-2-one compounds as mutant idh1 and idh2 inhibitors

Also Published As

Publication number Publication date
UA123640C2 (uk) 2021-05-05
CA3045303A1 (en) 2018-06-21
SI3555105T1 (sl) 2020-12-31
DK3555105T3 (da) 2020-11-09
MX2019006830A (es) 2019-08-22
WO2018111707A1 (en) 2018-06-21
ES2835281T3 (es) 2021-06-22
AU2020260493A1 (en) 2020-11-26
EA036112B1 (ru) 2020-09-29
MA53881A (fr) 2022-04-27
EP3763717B1 (en) 2023-03-08
JP2020502157A (ja) 2020-01-23
JOP20190142B1 (ar) 2023-03-28
JOP20190142A1 (ar) 2019-06-13
US11649247B2 (en) 2023-05-16
MA47399A (fr) 2019-10-23
US20200079791A1 (en) 2020-03-12
LT3555105T (lt) 2021-01-11
US11001596B2 (en) 2021-05-11
US20210206780A1 (en) 2021-07-08
AU2017378060A1 (en) 2019-05-30
JP6793836B2 (ja) 2020-12-02
KR20190077539A (ko) 2019-07-03
ES2941631T3 (es) 2023-05-24
US11629156B2 (en) 2023-04-18
CR20190252A (es) 2019-08-26
RS61108B1 (sr) 2020-12-31
PL3555105T3 (pl) 2021-05-17
AU2020260493B2 (en) 2021-09-09
CN115109075B (zh) 2024-09-20
HRP20201882T1 (hr) 2021-01-22
ECSP19042682A (es) 2019-06-30
EP3555105A1 (en) 2019-10-23
CN110072867A (zh) 2019-07-30
EA201991161A1 (ru) 2019-11-29
CN115109075A (zh) 2022-09-27
CY1123577T1 (el) 2022-03-24
KR102276022B1 (ko) 2021-07-13
MY197313A (en) 2023-06-13
MD3555105T2 (ro) 2021-01-31
CN110072867B (zh) 2022-07-08
CL2019001551A1 (es) 2019-10-25
MA47399B1 (fr) 2021-02-26
AU2017378060B2 (en) 2020-09-03
EP3763717A1 (en) 2021-01-13
PH12019501328A1 (en) 2020-02-24
SA519401897B1 (ar) 2022-07-28
CO2019005287A2 (es) 2019-05-31
BR112019009648A2 (pt) 2019-09-10
CA3045303C (en) 2022-05-17
HUE052067T2 (hu) 2021-04-28
IL267236B (en) 2020-08-31
ZA201903125B (en) 2024-08-28
US20210230185A1 (en) 2021-07-29
NZ754115A (en) 2021-07-30
TN2019000158A1 (en) 2020-10-05
DOP2019000163A (es) 2019-07-15
IL267236A (en) 2019-08-29
EP3555105B1 (en) 2020-10-28
PE20190977A1 (es) 2019-07-09

Similar Documents

Publication Publication Date Title
IL267236B (en) Derivatives of 7-phenylethylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one as 1idh and 2idh mutant inhibitors
IL279363A (en) PCSK9 antagonist compounds
ZA201802181B (en) 2¿phenyl¿3,4¿dihydropyrrolo[2,1 ¿f] [1,2,4]triazinone derivatives as phosphodiesterase inhibitors and uses thereof
EP3458445A4 (en) KRAS G12C INHIBITORS
EP3303382A4 (en) Compositions and methods for treating patients with rtk mutant cells
WO2017019429A8 (en) 7-phenylethylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one compounds and their use as mutant idh1 inhibitors
EP3091984A4 (en) Substituted benzoxazine and related compounds
EP3267998A4 (en) 3-substituted 1,3,4-oxadiazole and thiadiazole compounds as immunomodulators
HK1210609A1 (en) Fluoro-[1,3]oxazines as bace1 inhibitors bace1 -[13]
EP3389663A4 (en) PYRROLOPYRIMIDINE COMPOUNDS, USE AS LACKERS OF THE LRRK2 KINASE AND METHOD FOR THE PRODUCTION THEREOF
EP3364968A4 (en) OXAZOLIDINONE COMPOUNDS AND USES THEREOF AS ANTIBACTERIAL AGENTS
EP3268370A4 (en) Antimicrobial compounds and methods of making and using the same
EP3262174A4 (en) Compounds and methods for increasing antisense activity
EP3240768A4 (en) Nitrification inhibitor compositions and methods for preparing the same
EP3468555A4 (en) ANTIMICROBIAL CONNECTIONS AND METHOD FOR USE THEREOF
IL278701A (en) Heterofused pyridones and their use as IDH inhibitors
EP3355699A4 (en) BICYCLIC COMPOUND AND USE THEREOF FOR INHIBITION OF SUV39H2
EP3356357A4 (en) COMPOSITIONS AND METHODS OF INHIBITING BETA LACTAMASE
EP3568018A4 (en) COMPOUNDS AND METHOD OF USE
WO2014160628A3 (en) Articles and methods for preventing and treating dermatologic adverse events
EP3447138A4 (en) REGULATOR T CELL ACTIVATOR AND USE THEREOF
KR102383690B9 (ko) 벤족사진계 혼합물, 및 이의 용도
EP3364976A4 (en) PIPERAZINYL-NORBENZOMORPHAN COMPOUNDS AND METHOD FOR USE THEREOF
EP3192513A4 (en) 7-fluoro-8-chloro-5 -dibenzo[b,e][1,4]diazepine derivatives and use thereof
TH1501007226A (th) สารประกอบ 6,7-ไดไฮโดรไพราโซโล[1,5-a]ไพราซีน-4(5H)-โอน และการใช้ของ สิ่งนั้นในฐานะเป็นสารยับยั้งแอลโลสเตอริกของ mGluR2 รีเซ็ปเตอร์